Pages that link to "Q20196322"
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The following pages link to Cisca Wijmenga (Q20196322):
Displaying 50 items.
- Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (Q22251082) (← links)
- ImmunoChip study implicates antigen presentation to T cells in narcolepsy (Q23936601) (← links)
- Genetic variation in ICF syndrome: evidence for genetic heterogeneity (Q24290581) (← links)
- Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux (Q24300041) (← links)
- The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes (Q24302212) (← links)
- A novel role for XIAP in copper homeostasis through regulation of MURR1 (Q24302274) (← links)
- Characterization of COMMD protein-protein interactions in NF-kappaB signalling (Q24311936) (← links)
- Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter (Q24318590) (← links)
- Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease (Q24323378) (← links)
- Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea (Q24324212) (← links)
- Multiple common variants for celiac disease influencing immune gene expression (Q24608614) (← links)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (Q24609915) (← links)
- Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci (Q24618592) (← links)
- Shared and distinct genetic variants in type 1 diabetes and celiac disease (Q24623113) (← links)
- Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1 (Q24629883) (← links)
- Genome-wide association study of intracranial aneurysm identifies three new risk loci (Q24630663) (← links)
- Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection (Q24632121) (← links)
- Susceptibility loci for intracranial aneurysm in European and Japanese populations (Q24643743) (← links)
- Human dectin-1 deficiency and mucocutaneous fungal infections (Q24645008) (← links)
- Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes (Q24647056) (← links)
- The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome (Q24647294) (← links)
- A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (Q24649802) (← links)
- Newly identified genetic risk variants for celiac disease related to the immune response (Q24654340) (← links)
- The SPINK gene family and celiac disease susceptibility (Q24676700) (← links)
- Expressing the differences between Crohn disease and ulcerative colitis (Q24816928) (← links)
- Genome-wide association identifies multiple ulcerative colitis susceptibility loci (Q27865246) (← links)
- Gene expression profiling and phenotype analyses of S. cerevisiae in response to changing copper reveals six genes with new roles in copper and iron metabolism (Q27931265) (← links)
- The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression (Q28117183) (← links)
- The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis (Q28205001) (← links)
- A major non-HLA locus in celiac disease maps to chromosome 19 (Q28205703) (← links)
- The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein (Q28206233) (← links)
- The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis (Q28211287) (← links)
- Identification of a new copper metabolism gene by positional cloning in a purebred dog population (Q28216510) (← links)
- Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling (Q28236179) (← links)
- Genetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genes (Q28237040) (← links)
- Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort (Q28241930) (← links)
- Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population (Q28248685) (← links)
- Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients (Q28249834) (← links)
- An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia (Q28250481) (← links)
- A functional candidate screen for coeliac disease genes (Q28251539) (← links)
- Coeliac disease and autoimmune disease-genetic overlap and screening (Q28266589) (← links)
- Genetic variation in Toll-like receptors and disease susceptibility (Q28267031) (← links)
- Genetic variation in myosin IXB is associated with ulcerative colitis (Q28272638) (← links)
- Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect (Q28281383) (← links)
- Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort (Q28281845) (← links)
- Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci (Q28281906) (← links)
- Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease (Q28286971) (← links)
- Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations (Q28288723) (← links)
- Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function (Q28392223) (← links)
- Evaluation of European coeliac disease risk variants in a north Indian population (Q28395308) (← links)